A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3579176



Internal ID18530771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:32543594..32690290hg38UCSC Ensembl
Innerchr2:32768661..32915357hg19UCSC Ensembl
Innerchr2:32622165..32768861hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38146697
hg19146697
hg18146697
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005682
Supporting Variants
Samples
Known GenesBIRC6, MIR4765, TTC27
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3579176
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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